Clinical Trial Administrator Opportunity

Clinical Trial Administrator Opportunity

Job Title: Clinical Trial Administrator Opportunity
Contract Type: Permanent
Location: Horsham
Salary: To £35,000
Start Date: ASAP
Reference: 15912 BT
Contact Name: Brian Tappy
Contact Email:
Job Published: June 19, 2018 15:39

Job Description

To be based in Horsham, West Sussex – as an experienced CTA you will appreciate how vital the supply chain is to the success of any study. Central to all clinical trials is ensuring the correct doses are available for the correct patient and that they are transported under the correct conditions. Without a robust supply chain there would be no clinical trial be it a single center phase 1 or a global phase 3 study.

This is a great opportunity to develop a career in the in-demand area Clinical Supply Chain Management. If you have worked as a Clinical Trial Administrator / Associate or a related clinical operational role such as a Clinical Research Associate, Data Associate / Manager, IxRS Project Coordinator/Manager, Clinical Trial Pharmacy Technician etc this could be the opportunity you have been looking for.

The Company

The company is the global market leader and innovator in the provision of clinical supply chain solutions meeting the requirements of studies across the world. As clinical trials require increasingly complex supply chain support, the company’s integrated solutions provide the global presence and flexibility to integrate into clients own operational and quality processes. The company has operations in across the globe backed by a global distribution infrastructure.

The Role
Based on your clinical trial expertise this role is to join the Clinical Supply Chain Optimisation team as a Clinical Supply Chain Manager at Associate level. The role focuses on supporting external clients and internal Clinical Supply Chain Managers in translating study needs into supply chain strategies. This includes the interpretation of protocols and client’s operating procedures that will be successfully interpreted into robust plans. You will assist in developing processes and procedures ensuring supply availability which will be achieved by forecasting, scheduling, operational coordination and risk management. You will have the ability to work with cross-functional teams for study management activities including internal Project Management colleagues and external CROs, IxRS providers, client clinical supply teams and client clinical operations teams.

Based on your clinical trial experience full training and mentoring will be provided with an ongoing commitment to your development and a clear, structured career path for future progression.    


- Highly competitive salary to £35,000

- Full training in Clinical Supply Chains based on clinical trial expertise

- On going development and clear, structured career path for progression

- Contributory pension scheme

- Bonus scheme

- Private health cover

- Childcare vouchers


The successful candidate will have a good understanding of clinical trial processes and procedures including regulatory standards. You could have gained your expertise working as a Clinical Trial Administrator, Clinical Trial Associate, Clinical Research Coordinator, Clinical Research Associate, Data Associate/Manager, IxRS Project Coordination, Clinical Supplies Pharmacy Technician or other role with broad clinical trial exposure. This experience could have been gained in a pharmaceutical / sponsor, service provider / CRO or NHS environment.